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Updated: Aug 27, 2025

In Silico Identification and Characterization of circRNAs During Host-Pathogen Interactions
Published on: October 21, 2022
[Circular RNA-encoded peptides and proteins: implications to cancer]
Shuang Ao Ke1, Shengnan Zhao1, Yu Liu1
1Institute of Biology and Medicine, College of Life Science and Health, Wuhan University of Science and Technology, Wuhan 430081, Hubei, China.
Abstract:
Circular RNA (circRNA) is a single-stranded circular closed RNA molecule formed from linear RNA through reverse splicing. circRNAs are stable, highly conserved, and tissue-specific. circRNAs can regulate physiological and pathological processes through various mechanisms such as formation of competing endogenous RNA and interaction with binding proteins. It has been recently revealed that circRNAs can be translated into peptides and proteins to participate in the initiation and development of cancer. circRNAs are promising diagnostic and prognostic markers for human cancers as well as potential drug targets for cancer therapy. This review summarized the research progresses related to circRNA-encoded peptides and proteins in a variety of cancers. These peptides and proteins are translated through two different mechanisms that depend on internal ribosome entry site and m6A, respectively. We also summarized the potential use of circRNA-encoded peptides and proteins in the diagnosis, treatment, prognosis and mechanistic studies of various cancers.
Insights
Circular RNAs (circRNAs) can be translated into cancer-fighting peptides and proteins. This review explores their roles in cancer diagnosis, prognosis, and therapy development.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- Circular RNAs (circRNAs) are stable, conserved RNA molecules with regulatory roles.
- Emerging evidence shows circRNAs can be translated into functional peptides and proteins.
- These circRNA-encoded molecules are implicated in cancer initiation and progression.
Purpose of the Study:
- To review research on circRNA-encoded peptides and proteins in various cancers.
- To summarize the mechanisms of circRNA translation into peptides/proteins.
- To highlight their potential in cancer diagnosis, treatment, and prognosis.
Main Methods:
- Literature review of studies on circRNA translation and cancer.
- Analysis of mechanisms including internal ribosome entry site (IRES) and m6A modification.
- Synthesis of findings on circRNA-encoded peptides/proteins in oncogenesis.
Main Results:
- CircRNAs can encode peptides and proteins via IRES-dependent and m6A-dependent translation.
- These molecules play roles in diverse cancer types.
- circRNA-encoded products show potential as diagnostic and prognostic biomarkers.
Conclusions:
- circRNA-encoded peptides and proteins represent a novel layer of gene regulation in cancer.
- They offer promising avenues for cancer diagnostics, therapeutics, and mechanistic studies.
- Further research is warranted to fully elucidate their clinical potential.
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